<code id='CA1911EF77'></code><style id='CA1911EF77'></style>
    • <acronym id='CA1911EF77'></acronym>
      <center id='CA1911EF77'><center id='CA1911EF77'><tfoot id='CA1911EF77'></tfoot></center><abbr id='CA1911EF77'><dir id='CA1911EF77'><tfoot id='CA1911EF77'></tfoot><noframes id='CA1911EF77'>

    • <optgroup id='CA1911EF77'><strike id='CA1911EF77'><sup id='CA1911EF77'></sup></strike><code id='CA1911EF77'></code></optgroup>
        1. <b id='CA1911EF77'><label id='CA1911EF77'><select id='CA1911EF77'><dt id='CA1911EF77'><span id='CA1911EF77'></span></dt></select></label></b><u id='CA1911EF77'></u>
          <i id='CA1911EF77'><strike id='CA1911EF77'><tt id='CA1911EF77'><pre id='CA1911EF77'></pre></tt></strike></i>

          
          WSS
          Alnylam headquarters
          Kristoffer Tripplaar/Sipa USA/AP

          Alnylam Pharmaceuticals said Thursday that sales of its treatments for rare diseases grew 43% in the second quarter compared to the year-ago period, as the biotech prepares for a key meeting with the Food and Drug Administration in September.

          Net product sales in the quarter were $306 million, led by Amvuttra, the company’s RNAi treatment for hereditary ATTR, with sales of $132 million, exceeding Wall Street forecasts. Sales of Onpattro, its older medicine for hereditary ATTR, were $91 million, slightly less than expectations.

          advertisement

          The FDA has scheduled a meeting of outside experts on Sept. 13 to discuss the company’s application to expand the indication for Onpattro to include ATTR-CM, a related condition that affects the heart. The FDA decision is due by Oct. 8. An expansion would open a much larger market for the drug than its current approval, which largely targets nerve-related damage.

          Unlock this article by subscribing to STAT+ and enjoy your first 30 days free!

          GET STARTED Log In

          Leave your comment

          Please enter your name
          Please enter your comment

          fashion